EP3497149A1 - Siloxanes réactifs et leurs procédés de préparation - Google Patents

Siloxanes réactifs et leurs procédés de préparation

Info

Publication number
EP3497149A1
EP3497149A1 EP17715480.4A EP17715480A EP3497149A1 EP 3497149 A1 EP3497149 A1 EP 3497149A1 EP 17715480 A EP17715480 A EP 17715480A EP 3497149 A1 EP3497149 A1 EP 3497149A1
Authority
EP
European Patent Office
Prior art keywords
general formula
radical
hydrogen
radicals
unsaturated organic
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
EP17715480.4A
Other languages
German (de)
English (en)
Other versions
EP3497149B1 (fr
Inventor
Michael Stepp
Leonie DEICHNER
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Wacker Chemie AG
Original Assignee
Wacker Chemie AG
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Wacker Chemie AG filed Critical Wacker Chemie AG
Publication of EP3497149A1 publication Critical patent/EP3497149A1/fr
Application granted granted Critical
Publication of EP3497149B1 publication Critical patent/EP3497149B1/fr
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
    • C08G77/04—Polysiloxanes
    • C08G77/06—Preparatory processes
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
    • C07F7/02—Silicon compounds
    • C07F7/08—Compounds having one or more C—Si linkages
    • C07F7/18—Compounds having one or more C—Si linkages as well as one or more C—O—Si linkages
    • C07F7/1804—Compounds having Si-O-C linkages
    • C07F7/1872—Preparation; Treatments not provided for in C07F7/20
    • C07F7/1892—Preparation; Treatments not provided for in C07F7/20 by reactions not provided for in C07F7/1876 - C07F7/1888
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
    • C08G77/04—Polysiloxanes
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
    • C08G77/04—Polysiloxanes
    • C08G77/12—Polysiloxanes containing silicon bound to hydrogen
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
    • C08G77/04—Polysiloxanes
    • C08G77/14—Polysiloxanes containing silicon bound to oxygen-containing groups
    • C08G77/18—Polysiloxanes containing silicon bound to oxygen-containing groups to alkoxy or aryloxy groups
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
    • C08G77/04—Polysiloxanes
    • C08G77/20—Polysiloxanes containing silicon bound to unsaturated aliphatic groups
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
    • C08G77/04—Polysiloxanes
    • C08G77/22—Polysiloxanes containing silicon bound to organic groups containing atoms other than carbon, hydrogen and oxygen
    • C08G77/24—Polysiloxanes containing silicon bound to organic groups containing atoms other than carbon, hydrogen and oxygen halogen-containing groups

Definitions

  • the invention relates to reactive siloxanes having a backbone of organotrifunctional siloxane units and to a process for their preparation from lithium or sodium salts of
  • Organosilanols also referred to below as siliconates
  • halosilanes Organosilanols
  • T stands for RSiO 3/2 and M for R 3 Si0 1/2
  • T stands for RSiO 3/2 and M for R 3 Si0 1/2
  • a pure TM polysiloxane may have a maximum chain length of 17 (t ⁇ 15 in general formula (2))
  • the polymers of the invention excluded.
  • the described polysiloxanes Bl contain no SiH radicals.
  • WO 01/27187 (University of Southern California, 2000) claims a process for the preparation of branched polysiloxanes similar to those of the general formula (1) by anionic or cationic ring-opening polymerization of monosilyl-substituted cyclotrisiloxanes which are complicated to prepare.
  • this method does not allow fully silyl-substituted linear T-polymers because only every third siloxane unit in the chain is trifunctional.
  • Macromolecules 2000, 33, 6310-14 give access to polysiloxanes having a backbone of T units, which are also prepared by anionic ring-opening polymerization from the corresponding
  • T 3 M 3 cycle are accessible.
  • a disadvantage of this method is in addition to the elaborate preparation of the T-cycle and the technically difficult to implement process of anionic
  • No. 2567110 describes the reaction of a sodium methylsiliconate with trimethylchlorosilane (Ex. 1, column 6). Only cyclic structures can be deduced from the theoretical average siliconate salt structure formulated in column 2, line 32 for a metal: Si ratio of 1: 1. For metal Si ratios ⁇ 1 are no structures for
  • the invention relates to a process for the preparation of linear siloxanes of the general formula (1) by reaction of lithium or sodium salts of
  • n for a number from 3 to 100
  • R is an organic radical attached via carbon
  • R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 and R 9 independently represent a hydrogen radical or an organic over
  • Carbon or oxygen-bonded radical with the proviso that at least two radicals per molecule of the general formula (1) are selected from hydrogen and an aliphatically unsaturated organic radical.
  • the invention also relates to linear siloxanes of the general formula (1) in which
  • n for a number from 3 to 100
  • R is an organic radical bonded via carbon, R 1 , R 2 , R 3 , R 4 , R 5 and R 6 independently of one another
  • Hydrogen radical or an organic radical bound via carbon or oxygen Hydrogen radical or an organic radical bound via carbon or oxygen
  • radicals per molecule of the general formula (1) are selected from hydrogen and an aliphatically unsaturated organic radical and
  • Siliconate A is
  • the linear siloxanes of the general formula (1) can be any linear siloxanes of the general formula (1).
  • crosslinker e.g. for optical and electronic applications
  • functional fluids e.g. surface-active compounds and as potential
  • the radical R is preferably a monovalent Si-C bonded unsubstituted or by halogen atoms, Ci- 6 alkyl, Ci_ 6 -aryl or C x _6 alkoxy or silyl groups substituted hydrocarbon radical having 1 to 30 carbon atoms, in which one or multiple, non-adjacent -CH 2 units may be replaced by groups -O-, or -S- and there is no direct SiC bond to an aromatic carbon radical.
  • the radical R can be linear, branched, cyclic, saturated or unsaturated.
  • R is particularly preferably a monovalent
  • Unsubstituted alkyl radicals, cycloalkyl radicals, alkenyl radicals and alkylaryl radicals are particularly preferred.
  • the hydrocarbon radical R has 1 to 8 carbon atoms.
  • methyl, ethyl, propyl, 3, 3, 3-trifluoropropyl, isobutyl ( 2-methylprop-1-yl), vinyl, n-hexyl, 1-phenylethyl, 2 - Phenylethyl, the 4-vinyl-1-phenyl and Isooctylrest (eg, 2,4,4-trimethylpent-l-ylrest), especially the methyl radical and the vinyl radical, in particular the methyl radical. It is also possible to use mixtures of different radicals R in the siliconate A of the general formula
  • R radicals are - (CH 2 0) 0 -R10, - (CH 2 CH 2 0) P -R 1X, and CH 2 CH (CH 3) O) q -R 12 wherein o, p and q Values from 1 to 10, in particular 1, 2, 3 mean.
  • R 10 , R 11 and R 12 are preferably one
  • Alkyl radical having 1 to 6 carbon atoms examples include the methyl, the ethyl, the propyl, the allyl and the butyl radical, the methyl radical being particularly preferred.
  • index m is' preferably at least 0.1, more preferably at least 0.4, in particular at least 0.5 and at most 1.2, preferably at most 1.1, in particular 1.0.
  • index m is' preferably at least 0.1, more preferably at least 0.4, in particular at least 0.5 and at most 1.2, preferably at most 1.1, in particular 1.0.
  • mixtures of sodium and lithium cations and, in proportions of not more than 10 mol%, other metal cations may also occur.
  • the preparation of the siliconates according to the invention is preferably carried out according to the methods described in WO2013 / 041385, WO2012 / 022544,
  • the radicals R 1 to R 9 are preferably the hydrogen, a Ci_i 0 -alkoxy, a C 6 -2o-aryloxy or a monovalent
  • Silyl-substituted hydrocarbon radical having 1 to 18 carbon atoms Particularly preferred are hydrogen, C ⁇ -s ⁇ alkoxy, C 6 -io aryloxy and unsubstituted Cx-io-alkyl, C 3 _ 8 cycloalkyl, C 7-2 i-alkylaryl, C 7-2 i- Arylalkyl radicals and phenyl radicals.
  • Particularly preferred are hydrogen, C ⁇ -s ⁇ alkoxy, C 6 -io aryloxy and unsubstituted Cx-io-alkyl, C 3 _ 8 cycloalkyl, C 7-2 i-alkylaryl, C 7-2 i- Arylalkyl radicals and phenyl radicals.
  • radicals R 1 to R 9 are: 2-propyl
  • Radicals particularly preferably at least three radicals per molecule of the general formula (1) aliphatically unsaturated organic radicals and no radical means hydrogen. Preferred are
  • Alkenyl radicals especially vinyl and allyl radicals.
  • At least two radicals are hydrogen and no radical denotes aliphatically unsaturated organic radicals.
  • At least one radical are aliphatically unsaturated organic radicals and at least one radical, more preferably at least two radicals per molecule of hydrogen.
  • Preferred aliphatically unsaturated organic radicals are alkenyl radicals, in particular vinyl and allyl radicals.
  • the halosilanes are the halosilanes.
  • chlorosilanes of the general formula (3) are examples of chlorosilanes of the general formula (3).
  • Me 3 SiCl, HSiMe 2 Cl and ViSiMe 2 Cl Due to the manufacturing process, impurities due to organodiproducts and trihalosilanes can be present, especially in the technical qualities. However, their content preferably does not exceed 10 mol%.
  • the halosilanes are preferably prepared in the methylchlorosilane synthesis by the Muller-Rochow process, or can be prepared as secondary products by chemical reactions by known methods (e.g., hydrosilylation, nucleophilic substitution, radical substitution), and are most commonly available commercially.
  • the compounds of the general formula (1) are obtained by the process according to the invention by reacting one or more siliconates A with one or more halosilanes of the general formula (3). This can be done by adding the siliconate A to the halosilane or vice versa by adding the halosilane to the siliconate A. It lies
  • halosilanes are liquid at room temperature under normal pressure, the
  • Siliconate A solid It therefore makes sense to solve the siliconate A in an inert solvent or slurried and to meter in the liquid halogenated silanes neat or dissolved in an inert solvent in order to ensure the fastest possible reaction due to the good mixing.
  • Solvents are preferably aprotic polar and nonpolar organic solvents are used, for example, linear, branched or cyclic alkanes such as n-pentane, n-hexane, n-heptane, n-octane, isohexane, isooctane, cyclohexane, aromatics such as benzene, toluene, o- Xylene, m-xylene, p-xylene, ethers, such as diethyl ether, di-n-propyl ether, di-n-butyl ether, methyl t-butyl ether, phenylmethyl ether, diphenyl ether, tetrahydrofuran, 2-methyltetrahydrofuran, dioxane, tetrahydropyran, 4-methyltetrahydropyran, ethylene glycol dimethyl ether,
  • Diethylene glycol dimethyl ether diethylene glycol dimethyl ether, triethylene glycol dimethyl ether, ethylene glycol dibutyl ether, polyethylene glycols or
  • Polypropylene glycols or polybutylene glycols or glycol copolymers of different molecular weights / degrees of polymerization or siloxanes such as hexamethyldisiloxane, octamethyltrisiloxane, octamethylcyclotetrasiloxane, decamethylcyclopentasiloxane, methyltris-trimethylsiloxysilane or mixtures of various solvents.
  • Hydrogen halide can be added to an auxiliary base.
  • auxiliary base basic salts or nitrogenous
  • nitrogen-containing compounds examples include ammonia, ethylamine, butylamine, trimethylamine,
  • Nitrogen atoms do not carry hydrogen.
  • the auxiliary base is used at least equimolar with respect to the halosilane.
  • at least 0.5, more preferably at least 1.0, more preferably at least 2.0 base equivalents of auxiliary base are used per mole equivalent of halosilane. There may also be larger amounts added
  • Auxiliary base can be used - e.g. if this is to serve as a solvent at the same time. However, this usually brings no advantage, but reduces the space-time yield and thus the efficiency of the process.
  • the auxiliary base can be used - e.g. if this is to serve as a solvent at the same time. However, this usually brings no advantage, but reduces the space-time yield and thus the efficiency of the process.
  • the auxiliary base can be used - e.g. if this is to serve as a solvent at the same time.
  • this usually brings no advantage, but reduces the space-time yield and thus the efficiency of the process.
  • Auxiliary base is submitted. It is also possible to use mixtures of different auxiliary bases.
  • the siliconate A is reacted directly with the halosilane of the general formula (3) without auxiliary base and without solvent. If the siliconate A contains free SiOH groups, which in the
  • gaseous hydrogen halide may develop this
  • the siliconate A is optionally dispersed in an inert
  • Solvent preferably dosed to the halosilane.
  • the halosilane of the general formula (3) is used at least equimolar with respect to the siliconate A.
  • Per mole of siliconate silicon equivalent are preferably
  • per mole equivalent of siliconate A at most 30 molar equivalents, more preferably 10 molar equivalents, in particular at most 6 molar equivalents of halosilane
  • Siloxanes of the general formula (1) at least 2
  • addition-crosslinkable units This statistically means either at least 2 Si-bonded hydrogen radicals or at least 2 aliphatically unsaturated, preferably vinyl radicals, or at least one Si-bonded hydrogen radical and at least one aliphatic unsaturated, preferably vinyl radical. While the aliphatically unsaturated radicals can be introduced both via the siliconate A of the general formula (2) and via the halosilane of the general formula (3), the introduction of Si-bonded hydrogen radicals is possible only via the halosilane of the general formula (3).
  • the reaction of the siliconate A with the halosilane of the general formula (3) is preferably carried out at a temperature of at least -20 ° C, particularly preferably at least 0 ° C, in particular at least 10 ° C.
  • the reaction temperature preferably does not exceed 200 ° C., more preferably the reaction temperatures are at a maximum of 120 ° C., in particular not more than 70 ° C.
  • reaction mixture can both be cooled and heated, it is also possible to bring individual components to a specific temperature before they come into contact with one another, e.g. to use the heat of reaction.
  • the process can be carried out batchwise, e.g. in a stirrer as well as continuously e.g. be carried out in a loop or tubular reactor or a fluidized bed reactor or a paddle dryer. If the siliconate A as a solid or
  • Suspension is metered, this can be done via a solids sluice (for example screw conveyor or rotary valve).
  • a solids sluice for example screw conveyor or rotary valve.
  • Siloxanes are formed. In most cases it can be on the
  • the halide salts formed from the siliconate and from the optionally used auxiliary base during the reaction can be filtered off, decanted off, centrifuged off or dissolved in water and separated off as an aqueous solution.
  • aqueous workup can additionally a solvent
  • the aqueous work-up prior to the separation of the siloxane of the general formula (1) according to the invention is unfavorable when the siloxane of the general formula (1) bears particularly moisture-sensitive radicals, e.g.
  • Chlorosilane preferable.
  • the composition of the polysiloxanes according to the invention can be very well elucidated by means of 29 Si NMR spectroscopy.
  • the integration ratio of TM 2 end groups to TM units of the chain allows the average chain lengths and so that the average molecular weights can be easily determined.
  • the average chain length can be determined, for example, by the method of
  • the index n in the general formula (1) is preferably at least 5, more preferably at least 10, in particular at least 30, it is preferably not more than 90, more preferably not more than 70, in particular not more than 60.
  • Hydrogen still mean aliphatically unsaturated organic radical.
  • siloxanes of the general formula (1) are preferably prepared by the process according to the invention:
  • Formulas is the silicon atom tetravalent.
  • Lithium trifluoroacetate Lithium trifluoroacetate
  • Csl also calibrates internally, resulting in a mass variance of only 5 ppm.
  • mass deviations of up to 20 ppm are possible. From the mixture, 1 pL is applied to a stainless steel target, air dried and measured. The homologous series are more linear
  • Isopar ® E isoparaffinic hydrocarbon mixture with a boiling range of 113-143 ° C, commercially available from
  • Trimethylchlorosilane / dimethylchlorosilane mixture (9: 1).
  • Lg of in Example 1 a) obtained Siliconatpulvers is (in a mixture of 11.2 g of Isopar ® E and 4g of pyridine Merck KGaA,> 99.5%) at 23 ° C submitted.
  • To this suspension is a Mixture of 3.6 g of trimethylchlorosilane (technical grade, > 99%, WACKER CHEMIE AG) and 0.35 g of dimethylchlorosilane (techn.
  • Hexamethyldisiloxane and 1, 1, 3, 3 -Tetramethyldisiloxan find signals for the M 2 T end groups and MT chain fragments in a molar ratio of 1: 16.
  • the molar ratio H M: M units corresponds to that of the chlorosilanes used.
  • Hexamethyldisiloxane can be found signals for the M 2 T end groups and MT chain fragments in a molar ratio of 1: 23.5.
  • the molar ratio H M: M units corresponds to that of the chlorosilanes used.
  • demineralized water are added within 17 minutes. After 10 minutes, undissolved solids are filtered off and the two liquid phases are separated. The aqueous phase has a pH of 5. The clear, colorless organic phase is concentrated to 100 ° C / lhPa on a rotary evaporator. It then left 222.8 g of a clear, colorless viscous liquid.
  • Example 2 a 1 g of the Siliconatpulvers obtained in Example 2 a) is initially charged in a mixture of 11.2 g of Isopar ® E and 4 g of pyridine at 23 ° C. To this suspension are 4 g
  • Example 6 a 1 g of the Siliconatpulvers obtained in Example 6 a) is initially charged in a mixture of 11.2 g of Isopar ® E and 4 g of pyridine at 23 ° C. To this suspension are 4 g
  • demineralized water are added. After 30 minutes, the mixture is filtered and a 29 SiNMR spectrum taken from the upper organic phase of the filtrate. In addition to the signal for vinyldimethylsilanol, signals for the M 2 T end groups and MT chain fragments are found in a molar ratio of 1: 29.2.
  • Example 7 a 1 g of the Siliconatpulvers obtained in Example 7 a) is initially charged in a mixture of 11.2 g of Isopar ® E and 4 g of pyridine at 23 ° C. To this suspension are 4 g
  • demineralized water are added. After 30 minutes, the mixture is filtered and a 29 SiNMR spectrum taken from the upper organic phase of the filtrate. In addition to the signal for vinyldimethylsilanol, signals for the M 2 T end groups and MT chain fragments are found in a molar ratio of 1: 12.5.
  • Example 8 a 1 g of the Siliconatpulvers obtained in Example 8 a) is initially charged in a mixture of 11.2 g of Isopar ® E and 4 g of pyridine at 23 ° C. To this suspension are 4 g
  • Vinyldimethylchlorosilane (technical grade,> 98%, WACKER CHEMIE AG) added dropwise.
  • the white suspension is allowed to stir for 20 hours at room temperature (about 23 ° C) before adding 7 g of demineralized water. After 30 minutes, the mixture is filtered and a 29 SiNMR spectrum taken from the upper organic phase of the filtrate.
  • signals for the M 2 T end groups and MT chain fragments are found in a molar ratio of 1: 4.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Silicon Polymers (AREA)

Abstract

L'invention a pour objet des sixolanes (1) linéaires de formule générale:R1R2R3SiO- [R-Si (OSiR4R5R6) O]n-SiR1R2R3 , n représentant un nombre de 3 à 100, R un radical organique lié par le carbone, R1, R2, R3, R4, R5 et R6 réprésentant indépendamment les uns des autres un radical hydrogène ou un radical organique lié par le carbone ou l'oxygène, à condition, qu'au moins deux radicaux par molécule de formule générale (1) soient choisis parmi l'hydrogène et un radical organique à insaturation aliphatique et que, même si aucun des radicauxR1, R2, R3 ne représente l'hydrogène ou un radical organique à insaturation aliphatique, qu'il existe au moins une unité (OSiR4R5R6) dans laquelle les radicaux R4, R5, R6 ne sont ni l'hydrogène ni des radicaux organiques à insaturation aliphatique. Ceci concerne également leur production et leur utilisation.
EP17715480.4A 2017-04-04 2017-04-04 Siloxanes réactifs et leurs procédés de préparation Active EP3497149B1 (fr)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
PCT/EP2017/058013 WO2018184668A1 (fr) 2017-04-04 2017-04-04 Siloxanes réactifs et leurs procédés de préparation

Publications (2)

Publication Number Publication Date
EP3497149A1 true EP3497149A1 (fr) 2019-06-19
EP3497149B1 EP3497149B1 (fr) 2020-06-24

Family

ID=58489016

Family Applications (1)

Application Number Title Priority Date Filing Date
EP17715480.4A Active EP3497149B1 (fr) 2017-04-04 2017-04-04 Siloxanes réactifs et leurs procédés de préparation

Country Status (6)

Country Link
US (1) US10934396B2 (fr)
EP (1) EP3497149B1 (fr)
JP (1) JP6786716B2 (fr)
KR (1) KR102264716B1 (fr)
CN (1) CN109843982B (fr)
WO (1) WO2018184668A1 (fr)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2022184271A1 (fr) 2021-03-05 2022-09-09 Wacker Chemie Ag Silice fonctionnalisée par siloxane
KR20240055105A (ko) 2021-09-29 2024-04-26 와커 헤미 아게 저실라놀 폴리유기실록산의 제조 방법

Family Cites Families (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2567110A (en) 1947-07-12 1951-09-04 Corning Glass Works Organopolysiloxanes prepared by the reaction of salts of silanols with halosilanes
NL105985C (fr) * 1957-08-17 1900-01-01
FR2721318B1 (fr) * 1994-06-20 1996-12-06 Rhone Poulenc Chimie Polymère silicié organominéral, son utilisation comme agent tensio-actif dans les compositions détergentes et compositions détergentes contenant ledit polymère.
US5637668A (en) * 1996-04-01 1997-06-10 Dow Corning Corporation Preparation of polyorganosiloxanes by interfacial polymerization
US6284906B1 (en) 1999-10-12 2001-09-04 University Of Southern California Cyclotrisiloxanes, new siloxane polymers and their preparation
WO2003024870A1 (fr) * 2001-09-18 2003-03-27 Chisso Corporation Derives silsesquioxane et procede de fabrication
US7053167B2 (en) * 2002-09-13 2006-05-30 Chisso Corporation Silsesquioxane derivative having functional group
US7241851B2 (en) * 2002-12-30 2007-07-10 Momentive Performance Materials Inc. Silicone condensation reaction
JP2005231355A (ja) 2004-01-23 2005-09-02 Shin Etsu Chem Co Ltd 剥離フィルム
DE102010031624A1 (de) 2010-07-21 2012-01-26 Wacker Chemie Ag Wasserlösliche Organosiliconatpulver
DE102011083109A1 (de) 2011-09-21 2013-03-21 Wacker Chemie Ag Verfahren zur Herstellung von Pulvern aus Alkalisalzen von Silanolen
DE102011086812A1 (de) 2011-11-22 2013-05-23 Wacker Chemie Ag Verfahren zur Herstellung von Feststoffen aus Alkalisalzen von Silanolen
DE102014201883A1 (de) * 2014-02-03 2015-08-06 Wacker Chemie Ag Polysiloxane mit methylengebundenen polaren Gruppen
DE102014205258A1 (de) * 2014-03-20 2015-09-24 Wacker Chemie Ag Verfahren zur Herstellung von Pulvern aus Alkalisalzen von Silanolen
DE102014209583A1 (de) 2014-05-20 2015-11-26 Wacker Chemie Ag Verfahren zur Herstellung von Pulvern aus Alkalisalzen von Silanolen
DE102014212698A1 (de) * 2014-07-01 2016-01-07 Wacker Chemie Ag Verfahren zur Herstellung von Siloxanen aus Alkalisalzen von Silanolen

Also Published As

Publication number Publication date
US10934396B2 (en) 2021-03-02
KR20190054125A (ko) 2019-05-21
KR102264716B1 (ko) 2021-06-14
WO2018184668A1 (fr) 2018-10-11
CN109843982A (zh) 2019-06-04
JP6786716B2 (ja) 2020-11-18
CN109843982B (zh) 2021-11-19
US20190359774A1 (en) 2019-11-28
JP2020513424A (ja) 2020-05-14
EP3497149B1 (fr) 2020-06-24

Similar Documents

Publication Publication Date Title
EP2176319B1 (fr) Procédé pour produire des polysiloxanes ramifiés à fonctions sih
EP2159248B1 (fr) Procédé de fabrication de polysiloxanes fonctionnels SiH ramifiés et leur utilisation pour la fabrication de polysiloxanes organomodifiés ramifiés, connexes SiC ou SiOC et liquides
DE4205201B4 (de) Verfahren zur Herstellung von Organopolysiloxanen
EP3164407B1 (fr) Procédé de production de siloxanes à partir de sels alcalins de silanols
EP0927733A1 (fr) Méthode de préparation de polymères organo-siliciés comportant des motifs siloxanes mono et tetrafonctionnels
DE2849092A1 (de) Silylphosphate und verfahren zu deren herstellung
EP2540763B1 (fr) Procédé destiné à la fabrication d'organopolysiloxanes
EP0776935B1 (fr) Composés siliciques à bas poids moléculaire, procédé pour leur préparation et leur emploi dans les compositions d'organopolysiloxan réticulables
WO2013127774A1 (fr) Matières réticulables à base de composés organosiliciés
DE1745342B2 (de) Lineare Organopolysiloxane
EP3497149B1 (fr) Siloxanes réactifs et leurs procédés de préparation
DE4317978A1 (de) Organosiliciumreste aufweisende Phosphazene, Verfahren zu deren Herstellung und deren Verwendung
EP3221385B1 (fr) Procédé de préparation de siloxanols à partir de sels métalliques de silanols
DE4243895A1 (de) Verfahren zur Herstellung von Organopolysiloxanharz
EP2598556A1 (fr) Procédé de production de copolymères de siloxane avec des groupes de composés uréthane-sulfonamido
DE2331677C2 (de) Verfahren zur Herstellung von äqulllbrlerter Organopolysiloxangemische mit am Silicium gebundenen Organosulfonsäuregruppen
EP1544252B1 (fr) Compositions à base de composés organosiliciés stables au stockage
DE102014200106B4 (de) Härtbare organomodifizierte Siloxane hergestellt durch Kondensation
EP0948501A1 (fr) Composes organosiliciques comportant des groupes uree, leur procede de preparation et leur utilisation
WO2022083851A1 (fr) Procédé de synthèse d'aminosiloxanes contenant des groupes alcoxy
EP0538868A1 (fr) Composés organosiliciés comportant des groupes de sel de Bunte, leur procédé de préparation et leur utilisation

Legal Events

Date Code Title Description
STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: UNKNOWN

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE INTERNATIONAL PUBLICATION HAS BEEN MADE

PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: REQUEST FOR EXAMINATION WAS MADE

17P Request for examination filed

Effective date: 20190315

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR

GRAP Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOSNIGR1

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: GRANT OF PATENT IS INTENDED

INTG Intention to grant announced

Effective date: 20200224

GRAS Grant fee paid

Free format text: ORIGINAL CODE: EPIDOSNIGR3

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE PATENT HAS BEEN GRANTED

AK Designated contracting states

Kind code of ref document: B1

Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR

REG Reference to a national code

Ref country code: GB

Ref legal event code: FG4D

Free format text: NOT ENGLISH

REG Reference to a national code

Ref country code: CH

Ref legal event code: EP

REG Reference to a national code

Ref country code: DE

Ref legal event code: R096

Ref document number: 502017005862

Country of ref document: DE

REG Reference to a national code

Ref country code: AT

Ref legal event code: REF

Ref document number: 1283836

Country of ref document: AT

Kind code of ref document: T

Effective date: 20200715

REG Reference to a national code

Ref country code: IE

Ref legal event code: FG4D

Free format text: LANGUAGE OF EP DOCUMENT: GERMAN

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: SE

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200624

Ref country code: NO

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200924

Ref country code: GR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200925

Ref country code: FI

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200624

Ref country code: LT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200624

REG Reference to a national code

Ref country code: LT

Ref legal event code: MG4D

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: LV

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200624

Ref country code: HR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200624

Ref country code: BG

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200924

Ref country code: RS

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200624

REG Reference to a national code

Ref country code: NL

Ref legal event code: MP

Effective date: 20200624

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: NL

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200624

Ref country code: AL

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200624

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: EE

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200624

Ref country code: SM

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200624

Ref country code: IT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200624

Ref country code: PT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20201026

Ref country code: ES

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200624

Ref country code: CZ

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200624

Ref country code: RO

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200624

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: PL

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200624

Ref country code: SK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200624

Ref country code: IS

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20201024

REG Reference to a national code

Ref country code: DE

Ref legal event code: R097

Ref document number: 502017005862

Country of ref document: DE

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: DK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200624

PLBE No opposition filed within time limit

Free format text: ORIGINAL CODE: 0009261

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT

26N No opposition filed

Effective date: 20210325

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: SI

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200624

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: MC

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200624

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: LU

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20210404

REG Reference to a national code

Ref country code: BE

Ref legal event code: MM

Effective date: 20210430

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: CH

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20210430

Ref country code: LI

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20210430

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: IE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20210404

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: IS

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20201024

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: BE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20210430

P01 Opt-out of the competence of the unified patent court (upc) registered

Effective date: 20230510

REG Reference to a national code

Ref country code: AT

Ref legal event code: MM01

Ref document number: 1283836

Country of ref document: AT

Kind code of ref document: T

Effective date: 20220404

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: CY

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200624

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: HU

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT; INVALID AB INITIO

Effective date: 20170404

Ref country code: AT

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20220404

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: FR

Payment date: 20230424

Year of fee payment: 7

Ref country code: DE

Payment date: 20230420

Year of fee payment: 7

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: GB

Payment date: 20230419

Year of fee payment: 7

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: MK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20200624